Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.573828
Title: New approaches for the stereoselective synthesis of N-heterocycles
Author: Daly, Mark
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 2012
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Abstract:
A stereoselective approach has been developed for the flexible synthesis of substituted 2-pyrrolidones and 2-piperidones. By employing the key Overman rearrangement, efficient transfer of stereochemistry was achieved, and an acylation and ring closing metathesis strategy afforded a library of target N-heterocycles. In addition, the optimisation of a synthesis of 4-oxopipecolic acid derivatives from L-aspartic acid was investigated. A novel, milder and higher yielding 6-endo-trig cyclisation procedure was developed. This allowed for the generation of a library of 2,6-cis-substituted 4-oxopipecolic derivatives. Stereoselective carbonyl reduction extended the synthesis further to include 4-hydroxypipecolic acid derivatives.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.573828  DOI: Not available
Keywords: QD Chemistry
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